Lista de obras - Marcin W Wlodarski - Dominio Público Uruguay

A metabolic interplay coordinated by HLX regulates myeloid differentiation and AML through partly overlapping pathways

scientific article published in Nature Communications

Abnormal promoter DNA methylation in juvenile myelomonocytic leukemia is not caused by mutation in DNMT3A

scientific article published on 01 October 2011

Azacitidine is effective for targeting leukemia-initiating cells in juvenile myelomonocytic leukemia

scientific article published on 24 January 2019

CD4+CD25high Foxp3+ regulatory T cells in myelodysplastic syndrome (MDS).

artículo científico publicado en 2007

Changes in T-cell receptor VB repertoire in aplastic anemia: effects of different immunosuppressive regimens

artículo científico publicado en 2002

Classification of the biological material with use of FTIR spectroscopy and statistical analysis.

artículo científico publicado en 2010

Clonal PIGA mosaicism and dynamics in paroxysmal nocturnal hemoglobinuria

artículo científico publicado en 2018

Clonal drift demonstrates unexpected dynamics of the T-cell repertoire in T-large granular lymphocyte leukemia

artículo científico publicado en 2011

Clonal predominance of CD8(+) T cells in patients with unexplained neutropenia

artículo científico publicado en 2008

Cytomegalovirus-specific regulatory and effector T cells share TCR clonality--possible relation to repetitive CMV infections

artículo científico publicado en 2011

DNA methylation in PRDM8 is indicative for dyskeratosis congenita

artículo científico publicado en 2016

Deep sequencing of the T-cell receptor repertoire in CD8+ T-large granular lymphocyte leukemia identifies signature landscapes

artículo científico publicado en 2013

Discrimination of T-cell subsets and T-cell receptor repertoire distribution.

artículo científico publicado en 2014

Double-negative regulatory T cells induce allotolerance when expanded after allogeneic haematopoietic stem cell transplantation

artículo científico publicado en 2008

Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FA

artículo científico publicado en 2011

Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes

artículo científico publicado en 2012

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

artículo científico publicado en 2018

GFI1(36N) as a therapeutic and prognostic marker for myelodysplastic syndrome

artículo científico publicado en 2016

Glucocorticoids improve erythroid progenitor maintenance and dampen Trp53 response in a mouse model of Diamond-Blackfan anaemia.

artículo científico publicado en 2015

Hemangioblastomas and neurogenic polyglobulia

scientific article published on 01 June 2013

Immunogenetic factors determining the evolution of T-cell large granular lymphocyte leukaemia and associated cytopenias.

artículo científico publicado en 2006

Killer immunoglobulin-like receptor genotype in immune-mediated bone marrow failure syndromes

artículo científico publicado en 2005

Large granular lymphocyte (LGL)-like clonal expansions in paroxysmal nocturnal hemoglobinuria (PNH) patients.

artículo científico publicado en 2005

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.

artículo científico publicado en 2016

Molecular TCR diagnostics can be used to identify shared clonotypes after allogeneic hematopoietic stem cell transplantation.

artículo científico publicado en 2004

Molecular analysis of TCR clonotypes in LGL: a clonal model for polyclonal responses.

artículo científico publicado en 2004

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

artículo científico publicado en 2009

PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia

artículo científico publicado en 2014

Pathologic clonal cytotoxic T-cell responses: nonrandom nature of the T-cell-receptor restriction in large granular lymphocyte leukemia

artículo científico publicado en 2005

Pathophysiology defined by altered signal transduction pathways: the role of JAK-STAT and PI3K signaling in leukemic large granular lymphocytes.

artículo científico publicado en 2006

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

artículo científico publicado en 2015

RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia.

artículo científico publicado en 2017

Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes

artículo científico

Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita

artículo científico publicado en 2018

Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway

artículo científico publicado en 2015

SNP array-based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes.

artículo científico publicado en 2011

STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia

artículo científico publicado en 2012

Shared and individual specificities of immunodominant cytotoxic T-cell clones in paroxysmal nocturnal hemoglobinuria as determined by molecular analysis

artículo científico publicado en 2004

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

artículo científico publicado en 2000

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

artículo científico publicado en 2012

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

scientific article published on 18 June 2020

T-large granular lymphocyte leukemia: current molecular concepts.

artículo científico publicado en 2006

Tricky B-usiness: hematogones in aplastic anemia

scientific article published on 01 December 2009

Lista de obras de Marcin W Wlodarski

A metabolic interplay coordinated by HLX regulates myeloid differentiation and AML through partly overlapping pathways

Abnormal promoter DNA methylation in juvenile myelomonocytic leukemia is not caused by mutation in DNMT3A

Azacitidine is effective for targeting leukemia-initiating cells in juvenile myelomonocytic leukemia

CD4+CD25high Foxp3+ regulatory T cells in myelodysplastic syndrome (MDS).

Changes in T-cell receptor VB repertoire in aplastic anemia: effects of different immunosuppressive regimens

Classification of the biological material with use of FTIR spectroscopy and statistical analysis.

Clonal PIGA mosaicism and dynamics in paroxysmal nocturnal hemoglobinuria

Clonal drift demonstrates unexpected dynamics of the T-cell repertoire in T-large granular lymphocyte leukemia

Clonal predominance of CD8(+) T cells in patients with unexplained neutropenia

Cytomegalovirus-specific regulatory and effector T cells share TCR clonality--possible relation to repetitive CMV infections

DNA methylation in PRDM8 is indicative for dyskeratosis congenita

Deep sequencing of the T-cell receptor repertoire in CD8+ T-large granular lymphocyte leukemia identifies signature landscapes

Discrimination of T-cell subsets and T-cell receptor repertoire distribution.

Double-negative regulatory T cells induce allotolerance when expanded after allogeneic haematopoietic stem cell transplantation

Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FA

Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes

GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML

GFI1(36N) as a therapeutic and prognostic marker for myelodysplastic syndrome

Glucocorticoids improve erythroid progenitor maintenance and dampen Trp53 response in a mouse model of Diamond-Blackfan anaemia.

Hemangioblastomas and neurogenic polyglobulia

Immunogenetic factors determining the evolution of T-cell large granular lymphocyte leukaemia and associated cytopenias.

Killer immunoglobulin-like receptor genotype in immune-mediated bone marrow failure syndromes

Large granular lymphocyte (LGL)-like clonal expansions in paroxysmal nocturnal hemoglobinuria (PNH) patients.

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.

Molecular TCR diagnostics can be used to identify shared clonotypes after allogeneic hematopoietic stem cell transplantation.

Molecular analysis of TCR clonotypes in LGL: a clonal model for polyclonal responses.

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia

Pathologic clonal cytotoxic T-cell responses: nonrandom nature of the T-cell-receptor restriction in large granular lymphocyte leukemia

Pathophysiology defined by altered signal transduction pathways: the role of JAK-STAT and PI3K signaling in leukemic large granular lymphocytes.

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia.

Recommendations on hematopoietic stem cell transplantation for inherited bone marrow failure syndromes

Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita

Ribosomal Protein Mutations Result in Constitutive p53 Protein Degradation through Impairment of the AKT Pathway

SNP array-based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes.

STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia

Shared and individual specificities of immunodominant cytotoxic T-cell clones in paroxysmal nocturnal hemoglobinuria as determined by molecular analysis

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

T-large granular lymphocyte leukemia: current molecular concepts.

Tricky B-usiness: hematogones in aplastic anemia